esv3648728
- Organism: Homo sapiens
- Study:estd216 (Kasak et al. 2015)
- Variant Type:copy number variation
- Method Type:SNP array
- Submitted on:GRCh37 (hg19)
- Variant Calls:1
- Validation:Not tested
- Clinical Assertions: Yes
- Region Size:43,160
- Description:PLEASE NOTE: The calls represented in this region now have equivalents in the study Clinical Structural Variants (nstd102). Please use the preferred nstd102 variant region accession for this variant; you can find it at top right under "Links to Other Resources" or in the mapping file provided here.
- Publication(s):Kasak et al. 2015
- Genome View
- Variant Region Details and Evidence
- Validation Information
- Clinical Assertions
- Genotype Information
Genome View
Select assembly:Overlapping variant regions from other studies: 198 SVs from 35 studies. See in: genome view
Overlapping variant regions from other studies: 198 SVs from 35 studies. See in: genome view
Variant Region Placement Information
| Variant Region ID | Placement Type | Score | Assembly | Assembly Unit | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| esv3648728 | Remapped | Perfect | GRCh38.p12 | Primary Assembly | First Pass | NC_000014.9 | Chr14 | 90,292,547 | 90,335,706 |
| esv3648728 | Submitted genomic | GRCh37 (hg19) | Primary Assembly | NC_000014.8 | Chr14 | 90,758,891 | 90,802,050 |
Variant Call Information
| Variant Call ID | Type | Method | Analysis | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|---|
| essv16463072 | duplication | SNP array | Probe signal intensity | not provided | ClinVar | SCV000191702 |
Variant Call Placement Information
| Variant Call ID | Placement Type | Score | HGVS | Assembly | Reciprocity | Sequence ID | Chr | Outer Start | Outer Stop |
|---|---|---|---|---|---|---|---|---|---|
| essv16463072 | Remapped | Perfect | NC_000014.9:g.(902 92547_?)_(?_903357 06)dup | GRCh38.p12 | First Pass | NC_000014.9 | Chr14 | 90,292,547 | 90,335,706 |
| essv16463072 | Submitted genomic | NC_000014.8:g.(907 58891_?)_(?_908020 50)dup | GRCh37 (hg19) | NC_000014.8 | Chr14 | 90,758,891 | 90,802,050 |
No validation data were submitted for this variant
Clinical Assertions
| Variant Call ID | HGVS | Type | Clinical Interpretation | Source of Interpretation | ClinVar ID |
|---|---|---|---|---|---|
| essv16463072 | GRCh37: NC_000014.8:g.(90758891_?)_(?_90802050)dup | duplication | not provided | ClinVar | SCV000191702 |